KR101784738B1 - Additive for electrolyte and electrolyte and lithium secondary battery - Google Patents

Abstract

상기 화학식 1에서, R¹ 내지 R⁴는 명세서에서 정의한 바와 같다.An electrolyte additive represented by the following general formula (1), an electrolyte, and a lithium secondary battery:
[Chemical Formula 1]

In Formula 1, R ¹ to R ⁴ are as defined in the specification.

Description

TECHNICAL FIELD [0001] The present invention relates to an electrolyte additive, an electrolyte solution, and a lithium secondary battery,

An electrolyte additive, an electrolyte, and a lithium secondary battery.

A battery is a device that converts the chemical energy generated by an electrochemical oxidation-reduction reaction of an internal chemical substance into electrical energy. When the energy inside the battery is exhausted, the primary battery and the rechargeable secondary battery . Among them, the secondary battery can be used by charging and discharging several times by using reversible conversion between chemical energy and electric energy.

On the other hand, the development of high-tech electronic industry has made it possible to miniaturize and lighten electronic equipment, and the use of portable electronic devices is increasing. The need for a battery having a high energy density as a power source for such portable electronic devices has been increased, and research on lithium secondary batteries has been actively conducted.

The lithium secondary battery includes a positive electrode including a positive electrode active material capable of intercalating and deintercalating lithium, a negative electrode including a negative active material capable of intercalating and deintercalating lithium, And the electrolyte solution is injected into the battery cell.

The electrolytic solution uses an organic solvent in which a lithium salt is dissolved and is important for determining the stability and performance of the lithium secondary battery.

One embodiment provides an electrolyte additive capable of improving performance while ensuring stability.

Another embodiment provides an electrolyte solution for a lithium secondary battery comprising the electrolyte additive.

Another embodiment provides a lithium secondary battery comprising the electrolytic solution.

According to one embodiment, there is provided an electrolyte additive represented by the following general formula (1).

[Chemical Formula 1]

In Formula 1,

Each of R ¹ to R ⁴ independently represents a hydrogen atom, a C1 to C12 alkyl group, a C1 to C12 alkenyl group, a C1 to C12 alkoxy group, a C1 to C12 oxalkyl group, a C6 to C20 aryloxy group, a halogen atom, alkyl group, a nitro group, C6 to C20 aryl group, a C2 to C20 heteroaryl group, C6 to C20 haloaryl group, -NR ⁵ R ⁶ (R ⁵ and R ⁶ are each independently an alkyl group, an alkenyl group, an aryl group, and oxazole is at least one selected from the group consisting of an alkyl group, R ⁵ and R ⁶ may form a ^{ring), R 7 -C (O)} -., R 7 -OC (O) -, R 7 -C (O ) -O-, R ⁷ -OC (O) -CH ₂ - (R ⁷ is at least one selected from the group consisting of an alkyl group, an aryl group, a fluoroalkyl group, a haloaryl group and a heteroaryl group) ion, and _{C n H 2n-1-m} (CN) m (n is an integer from 1 to 12, m is an integer from 1 to 6), -OR '(R' is a C1 to C12 alkyl group), and -R '' C (O) -OR '''(R''is a C1 to C4 alkyl group And R '''is a C1 to C12 alkyl group).

Wherein R ¹ and R ⁴ are each independently a hydrogen atom or a C 1 to C 12 alkyl group, and each of R ² and R ³ is independently -OR '(R' is a C 1 to C 12 alkyl group) or -R ' ) -OR '''(whereinR''is a C1 to C4 alkyl group and R''' is a C1 to C12 alkyl group).

For example, the formula (1) may be represented by the following formula (2) or (3).

(2)

(3)

In the above Formulas 2 and 3,

R 'and R' '' are each independently a C1 to C12 alkyl group and R '' is a C1 to C4 alkyl group.

The formula (1) may be represented by the following formula (4) or (5).

[Chemical Formula 4]

[Chemical Formula 5]

According to another embodiment, there is provided an electrolyte solution for a lithium secondary battery comprising a lithium salt, a non-aqueous organic solvent, and an electrolyte additive represented by the above formula (1).

The electrolyte additive may be represented by any one of the formulas (2) to (5).

The electrolyte additive may be included in an amount of about 0.001 to 5% by weight based on the total amount of the electrolytic solution.

The electrolyte additive may be included in an amount of about 0.01 to 2% by weight based on the total amount of the electrolytic solution.

According to another embodiment, there is provided a positive electrode comprising a positive electrode active material, a negative electrode including a negative electrode active material, and a lithium secondary battery including the above-described electrolyte.

The lithium secondary battery may further include a passivation film located on the surface of the anode.

By forming a stable passivation film on the surface of the positive electrode by the electrolyte additive, the performance of the battery can be improved and the flame retardancy can be increased to ensure stability.

FIG. 1 is a schematic view showing a lithium secondary battery according to one embodiment,
FIG. 2 is a graph showing decomposition potentials of an electrolytic solution in a half-cell according to Examples 3 and 4 and Comparative Examples 1 and 2,
3 is a graph showing a capacity retention rate according to cycles of a coin cell according to Example 6 and Comparative Example 4,
4 is a graph showing a capacity retention rate according to cycles of a coin cell according to Example 8 and Comparative Example 4,
5 is a graph showing capacity retention ratios according to cycles of coin cells according to Examples 7 and 9 and Comparative Examples 3 and 4,
6 is an LSV graph showing the results of current changes according to changes in applied voltages of Example 10 and Comparative Example 5. Fig.

Hereinafter, exemplary embodiments of the present invention will be described in detail so that those skilled in the art can easily carry out the present invention. The present invention may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein.

Unless otherwise defined herein, "substituted" means that the hydrogen atom in the compound is a halogen atom (F, Cl, Br or I), a hydroxy group, an alkoxy group, a nitro group, a cyano group, an amino group, A carboxyl group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid or a salt thereof, a C1 to C20 alkyl group, a C2 to C20 alkenyl group, a C2 to C20 alkenyl group, a C2 to C20 alkenyl group, C6 to C30 aryl groups, C7 to C30 arylalkyl groups, C1 to C20 alkoxy groups, C1 to C20 heteroalkyl groups, C3 to C20 heteroarylalkyl groups, C3 to C30 cycloalkyl groups, C3 to C15 cycloalkenyl groups, C6 to C20 aryl groups, C15 cycloalkynyl group, a C2 to C20 heterocycloalkyl group, and combinations thereof.

In addition, unless otherwise defined herein, "hetero" means containing 1 to 3 heteroatoms selected from N, O, S and P.

Hereinafter, an electrolyte additive according to one embodiment will be described.

The electrolyte additive according to one embodiment is a compound represented by the following formula (1).

[Chemical Formula 1]

In Formula 1,

Each of R ¹ to R ⁴ independently represents a hydrogen atom, a C1 to C12 alkyl group, a C1 to C12 alkenyl group, a C1 to C12 alkoxy group, a C1 to C12 oxalkyl group, a C6 to C20 aryloxy group, a halogen atom, alkyl group, a nitro group, C6 to C20 aryl group, a C2 to C20 heteroaryl group, C6 to C20 haloaryl group, -NR ⁵ R ⁶ (R ⁵ and R ⁶ are each independently an alkyl group, an alkenyl group, an aryl group, and oxazole is at least one selected from the group consisting of an alkyl group, R ⁵ and R ⁶ may form a ^{ring), R 7 -C (O)} -., R 7 -OC (O) -, R 7 -C (O ) -O-, R ⁷ -OC (O) -CH ₂ - (R ⁷ is at least one selected from the group consisting of an alkyl group, an aryl group, a fluoroalkyl group, a haloaryl group and a heteroaryl group) ion, and _{C n H 2n-1-m} (CN) m (n is an integer from 1 to 12, m is an integer from 1 to 6), -OR '(R' is a C1 to C12 alkyl group), and -R '' C (O) -OR '''(R''is a C1 to C4 alkyl group And R '''is a C1 to C12 alkyl group).

Wherein R ¹ and R ⁴ are each independently a hydrogen atom or a C 1 to C 12 alkyl group, and each of R ² and R ³ is independently -OR '(R' is a C 1 to C 12 alkyl group) or -R ' ) -OR '''(whereinR''is a C1 to C4 alkyl group and R''' is a C1 to C12 alkyl group).

Specifically, the electrolyte additive may be, for example, a compound represented by the following formula (2) or (3).

(2)

(3)

In the above Formulas 2 and 3,

R 'and R' '' are each independently a C1 to C12 alkyl group and R '' is a C1 to C4 alkyl group.

More specifically, the electrolyte additive may be a compound represented by the following general formula (4) or (5).

[Chemical Formula 4]

[Chemical Formula 5]

The electrolyte additive may be added to an electrolyte solution for a lithium secondary battery. The electrolyte additive not only improves the flame retardancy of the electrolyte solution to improve stability, but also causes a decomposition reaction on the surface of the anode to form a stable passivation film, thereby improving the life characteristics of the battery.

Hereinafter, an electrolyte solution for a lithium secondary battery according to one embodiment will be described.

The electrolyte for a lithium secondary battery according to an embodiment includes a lithium salt, a non-aqueous organic solvent, and an additive.

The lithium salt serves as a source of lithium ions in the battery to enable operation of a basic lithium secondary battery and to promote the movement of lithium ions between the positive electrode and the negative electrode. The lithium salt Representative examples are _{LiPF 6, LiBF 4, LiSbF 6} , LiAsF 6, LiN (SO 2 C 2 F 5) 2, Li (CF 3 SO 2) 2 N, LiN (SO 3 C 2 F 5) 2, _{LiCF 3 SO 3, LiC 4 F} 9 SO 3, LiClO 4, LiAlO 2, LiAlCl 4, LiC (CF 3 SO 2) 3, LiN (C x F 2x +1 SO 2) (C y F 2y +1 SO 2 ) (Where x and y are natural numbers), LiCl and LiI.

The concentration of the lithium salt is preferably within the range of 0.1M to 2.0M. When the concentration of the lithium salt is in the above range, the conductivity and viscosity of the electrolytic solution can be appropriately maintained, and excellent electrolyte performance can be exhibited, and lithium ions can be effectively moved.

The non-aqueous organic solvent serves as a medium through which ions involved in the electrochemical reaction of the battery can move.

The non-aqueous organic solvent may be a carbonate, ester, ether, ketone, alcohol, or aprotic solvent. Examples of the carbonate solvent include dimethyl carbonate (DMC), diethyl carbonate (DEC), dipropyl carbonate (DPC), methylpropyl carbonate (MPC), ethyl propyl carbonate (EPC), ethyl methyl carbonate (EMC) EC), fluoroethylene carbonate (FEC), propylene carbonate (PC), butylene carbonate (BC), etc. The ester solvents include methyl acetate, ethyl acetate, n- Propanolate, propionate, ethyl propionate, ethyl butyrate, gamma-butyrolactone, decanolide, gamma-valerolactone, mevalonolactone, caprolactone and the like can be used.

Examples of the ether solvent include dibutyl ether, tetraglyme, diglyme, dimethoxyethane, 2-methyltetrahydrofuran, and tetrahydrofuran. As the ketone solvent, cyclohexanone may be used have. As the alcoholic solvent, ethyl alcohol, isopropyl alcohol and the like can be used. As the aprotic solvent, R-CN (wherein R is a C2 to C20 linear, branched, or cyclic hydrocarbon group , A double bond aromatic ring or an ether bond); Amides such as dimethylformamide or dimethylacetamide, dioxolanes such as 1,3-dioxolane, and sulfolanes.

The non-aqueous organic solvent may be used alone or in admixture of one or more. If the non-aqueous organic solvent is used in combination, the mixing ratio may be appropriately adjusted according to the desired cell performance. .

In the case of the carbonate-based solvent, it is preferable to use a mixture of a cyclic carbonate and a chain carbonate. In this case, when the cyclic carbonate and the chain carbonate are mixed in a volume ratio of about 1: 1 to about 1: 9, the performance of the electrolytic solution may be excellent.

The non-aqueous organic solvent may further include an aromatic hydrocarbon-based organic solvent in the carbonate-based solvent. At this time, the carbonate-based solvent and the aromatic hydrocarbon-based organic solvent may be mixed in a volume ratio of about 1: 1 to about 30: 1.

Specific examples of the aromatic hydrocarbon-based organic solvent include benzene, fluorobenzene, 1,2-difluorobenzene, 1,3-difluorobenzene, 1,4-difluorobenzene, 1,2,3-tri Fluorobenzene, 1,2,4-trifluorobenzene, 1,2-dichlorobenzene, 1,3-dichlorobenzene, 1,4-dichlorobenzene, 1,2,3-trichlorobenzene, 1 , 2,4-trichlorobenzene, iodobenzene, 1,2-diiodobenzene, 1,3-diiodobenzene, 1,4-diiodobenzene, 1,2,3-triiodobenzene, Examples of the solvent include 2,4-triiodobenzene, toluene, fluorotoluene, 2,3-difluorotoluene, 2,4-difluorotoluene, 2,5-difluorotoluene, 2,3,4- Dichlorotoluene, 2,3-dichlorotoluene, 2,5-dichlorotoluene, 2,3,4-trichlorotoluene, 2, 3-dichlorotoluene, 3,5-trichlorotoluene, iodotoluene, 2,3-diiodotoluene, 2,4-diiodotoluene, 2 , 5-diiodotoluene, 2,3,4-triiodotoluene, 2,3,5-triiodotoluene, xylene, and combinations thereof.

The additive may be represented by the following general formula (1).

 [Chemical Formula 1]

In Formula 1,

Each of R ¹ to R ⁴ independently represents a hydrogen atom, a C1 to C12 alkyl group, a C1 to C12 alkenyl group, a C1 to C12 alkoxy group, a C1 to C12 oxalkyl group, a C6 to C20 aryloxy group, a halogen atom, alkyl group, a nitro group, C6 to C20 aryl group, a C2 to C20 heteroaryl group, C6 to C20 haloaryl group, -NR ⁵ R ⁶ (R ⁵ and R ⁶ are each independently an alkyl group, an alkenyl group, an aryl group, and oxazole is at least one selected from the group consisting of an alkyl group, R ⁵ and R ⁶ may form a ^{ring), R 7 -C (O)} -., R 7 -OC (O) -, R 7 -C (O ) -O-, R ⁷ -OC (O) -CH ₂ - (R ⁷ is at least one selected from the group consisting of an alkyl group, an aryl group, a fluoroalkyl group, a haloaryl group and a heteroaryl group) ion, and _{C n H 2n-1-m} (CN) m (n is an integer from 1 to 12, m is an integer from 1 to 6), -OR '(R' is a C1 to C12 alkyl group), and -R '' C (O) -OR '''(R''is a C1 to C4 alkyl group And R '''is a C1 to C12 alkyl group).

Wherein R ¹ and R ⁴ are each independently a hydrogen atom or a C 1 to C 12 alkyl group, and each of R ² and R ³ is independently -OR '(R' is a C 1 to C 12 alkyl group) or -R ' ) -OR '''(whereinR''is a C1 to C4 alkyl group and R''' is a C1 to C12 alkyl group).

The first additive may be a compound represented by any one of the following formulas (2) to (5).

(2)

(3)

[Chemical Formula 4]

[Chemical Formula 5]

In the above Formulas 2 and 3,

R 'and R' '' are each independently a C1 to C12 alkyl group and R '' is a C1 to C4 alkyl group.

The electrolyte additive not only improves the flame retardancy of the electrolyte solution to improve the stability, but also can form a stable passivation film by causing a decomposition reaction on the surface of the anode, thereby improving the lifetime characteristics of the battery.

The electrolyte additive may be included in an amount of about 0.001 to 5% by weight based on the total amount of the electrolytic solution. By being included in the above range, the flame retardancy can be effectively improved and a stable passivation film can be formed by decomposition on the electrode surface. The electrolyte additive may be included in the range of about 0.01 to 2% by weight.

Hereinafter, a lithium secondary battery according to another embodiment will be described with reference to the drawings.

1 is a schematic view showing a lithium secondary battery according to one embodiment.

1, a lithium secondary battery 100 according to an embodiment includes a cathode 112, a cathode 114 positioned opposite the cathode 112, and a cathode 112 disposed between the cathode 112 and the anode 114 (Not shown) for impregnating the separator 113 and the negative electrode 112, the positive electrode 114 and the separator 113, and a battery cell 120 containing the battery cell. And a sealing member 140 sealing the battery container 120.

The lithium secondary battery 100 may be manufactured by stacking a cathode 112, a separator 113 and an anode 114 in this order and then winding the battery in a spiral wound state in the battery container 120.

The cathode 112 includes a current collector and a negative electrode active material layer formed on the current collector.

The current collector may be a copper foil, a nickel foil, a stainless steel foil, a titanium foil, a nickel foil, a copper foil, a polymer substrate coated with a conductive metal, or a combination thereof.

The negative electrode active material layer includes a negative electrode active material, a binder, and optionally a conductive material.

The negative electrode active material includes a material capable of reversibly intercalating / deintercalating lithium ions, a lithium metal, an alloy of lithium metal, a material capable of doping and dedoping lithium, or a transition metal oxide.

As a material capable of reversibly intercalating / deintercalating lithium ions, any carbonaceous anode active material commonly used in lithium ion secondary batteries can be used as the carbonaceous material. Typical examples thereof include crystalline carbon , Amorphous carbon, or a combination thereof. Examples of the crystalline carbon include graphite such as natural graphite or artificial graphite in the form of amorphous, plate-like, flake, spherical or fibrous type. Examples of the amorphous carbon include soft carbon (soft carbon) Or hard carbon, mesophase pitch carbide, fired coke, and the like.

Examples of the lithium metal alloy include lithium and a metal such as Na, K, Rb, Cs, Fr, Be, Mg, Ca, Sr, Si, Sb, Pb, In, Zn, Ba, Alloys may be used.

As the material capable of doping and dedoping lithium, Si, SiO _x (0 <x <2), Si-C composite, Si-Q alloy (Q is an alkali metal, an alkaline earth metal, , transition metal, rare earth element or a combination of these, Si is not), Sn, SnO _2, Sn-C composite, Sn-R ⁸ (wherein R ⁸ is an alkali metal, alkaline earth metal, a Group 13 to 16 element, transition Metal, a rare earth element, or a combination thereof, but not Sn). The specific elements of Q and R ⁸ include Mg, Ca, Sr, Ba, Ra, Sc, Y, Ti, Zr, Hf, Rf, V, Nb, Ta, Db, Cr, Mo, W, , Re, Bh, Fe, Pb, Ru, Os, Hs, Rh, Ir, Pd, Pt, Cu, Ag, Au, Zn, Cd, B, Al, Ga, Sn, In, , Sb, Bi, S, Se, Te, Po, or a combination thereof.

Examples of the transition metal oxide include vanadium oxide, lithium vanadium oxide, and the like.

The binder serves to adhere the anode active material particles to each other and to adhere the anode active material to the current collector. Typical examples thereof include polyvinyl alcohol, carboxymethyl cellulose, hydroxypropyl cellulose, polyvinyl chloride, Such as polyvinyl chloride, polyvinyl fluoride, polymers comprising ethylene oxide, polyvinyl pyrrolidone, polyurethane, polytetrafluoroethylene, polyvinylidene fluoride, polyethylene, polypropylene, styrene-butadiene rubber, Styrene-butadiene rubber, epoxy resin, nylon, and the like may be used, but the present invention is not limited thereto.

The conductive material is used for imparting conductivity to the electrode. Any material can be used as long as it does not cause any chemical change in the battery. Examples of the conductive material include natural graphite, artificial graphite, carbon black, acetylene black, , Carbon-based materials such as carbon fibers; Metal powders such as copper, nickel, aluminum, and silver, or metal-based materials such as metal fibers; Conductive polymers such as polyphenylene derivatives; Or a mixture thereof may be used.

The anode 114 includes a current collector and a cathode active material layer formed on the current collector.

Al may be used as the current collector, but the present invention is not limited thereto.

The cathode active material layer includes a cathode active material, a binder, and optionally a conductive material.

As the cathode active material, a compound capable of reversibly intercalating and deintercalating lithium (a lithiated intercalation compound) can be used. Concretely, it is possible to use at least one of complex oxides of cobalt, manganese, nickel or a combination of metals and lithium, and specific examples thereof include compounds represented by any one of the following formulas. Li _a A _{1 - b} R _b D ₂ wherein, in the formula, 0.90? A? 1.8 and 0? B? 0.5; Li _a E _{1 - b} R _b O _{2 - c} D _c , wherein 0.90 ≤ a ≤ 1.8, 0 ≤ b ≤ 0.5, and 0 ≤ c ≤ 0.05; LiE _{2 - b} R _b O _{4 - c} D _{c where} 0? B? 0.5, 0? C? 0.05; Li _a Ni _{1 -b- c} Co _b R _c D _{α where} 0.90 ≦ a ≦ 1.8, 0 ≦ b ≦ 0.5, 0 ≦ c ≦ 0.05, and 0 <α ≦ 2; Li _a Ni _{1 - b - c} Co _b R _c O _{2 - ?} Z _{? Wherein} 0.90? A? 1.8, 0? B? 0.5, 0? C? 0.05 and 0 <? Li _a Ni _{1 -b- c} Co _b R _c O _{2 - ?} Z ₂ wherein 0.90? A? 1.8, 0? B? 0.5, 0? C? 0.05, and 0 <? Li _a Ni _1-bc Mn _b R _c D _? Wherein, in the formula, 0.90? A? 1.8, 0? B? 0.5, 0? C? 0.05 and 0 <? Li _a Ni _{1 -b- c} Mn _b R _c O _{2 - ?} Z _{? Where the} 0.90? A? 1.8, 0? B? 0.5, 0? C? 0.05 and 0 <? Li _a Ni _{1 -b- c} Mn _b R _c O _{2 - ?} Z ₂ wherein 0.90? A? 1.8, 0? B? 0.5, 0? C? 0.05 and 0 <? Li _a Ni _b E _c G _d O ₂ wherein 0.90 ≤ a ≤ 1.8, 0 ≤ b ≤ 0.9, 0 ≤ c ≤ 0.5, and 0.001 ≤ d ≤ 0.1; Li _a Ni _b Co _c Mn _d GeO ₂ wherein 0.90 ≤ a ≤ 1.8, 0 ≤ b ≤ 0.9, 0 ≤ c ≤ 0.5, 0 ≤ d ≤ 0.5, and 0.001 ≤ e ≤ 0.1; Li _a NiG _b O ₂ (in the above formula, 0.90? A? 1.8 and 0.001? B? 0.1); Li _a CoG _b O ₂ (in the above formula, 0.90? A? 1.8 and 0.001? B? 0.1); Li _a MnG _b O ₂ wherein, in the above formula, 0.90? A? 1.8 and 0.001? B? 0.1; Li _a Mn ₂ G _b O ₄ (in the above formula, 0.90? A? 1.8 and 0.001? B? 0.1); QO _2; QS ₂ ; LiQS ₂ ; V ₂ O ₅ ; LiV ₂ O ₅ ; LiTO ₂ ; LiNiVO _4; Li _(3-f) J ₂ (PO ₄ ) ₃ (0? F? 2); Li _(3-f) Fe ₂ (PO ₄ ) ₃ (0? F? 2); And LiFePO _4.

In the above formula, A is Ni, Co, Mn or a combination thereof; R is Al, Ni, Co, Mn, Cr, Fe, Mg, Sr, V, a rare earth element or a combination thereof; D is O, F, S, P or a combination thereof; E is Co, Mn or a combination thereof; Z is F, S, P or a combination thereof; G is Al, Cr, Mn, Fe, Mg, La, Ce, Sr, V or a combination thereof; Q is Ti, Mo, Mn or a combination thereof; T is Cr, V, Fe, Sc, Y or a combination thereof; J is V, Cr, Mn, Co, Ni, Cu or a combination thereof.

Of course, a compound having a coating layer on the surface of the compound may be used, or a compound having a coating layer may be mixed with the compound. The coating layer may comprise, as a coating element compound, an oxide, a hydroxide of a coating element, an oxyhydroxide of a coating element, an oxycarbonate of a coating element, or a hydroxycarbonate of a coating element. The compound constituting these coating layers may be amorphous or crystalline. The coating layer may contain Mg, Al, Co, K, Na, Ca, Si, Ti, V, Sn, Ge, Ga, B, As, Zr or a mixture thereof. The coating layer forming step may be carried out by any of coating methods such as spray coating, dipping, and the like without adversely affecting the physical properties of the cathode active material by using these elements in the above compound. It is a content that can be well understood by people engaged in the field, so detailed explanation will be omitted.

The binder serves to adhere the positive electrode active material particles to each other and to adhere the positive electrode active material to the current collector. Typical examples thereof include polyvinyl alcohol, carboxymethyl cellulose, hydroxypropyl cellulose, diacetyl cellulose, polyvinyl Polyvinylpyrrolidone, polyurethane, polytetrafluoroethylene, polyvinylidene fluoride, polyethylene, polypropylene, styrene-acrylonitrile, styrene-butadiene rubber, Butadiene rubber, acrylated styrene-butadiene rubber, epoxy resin, nylon, and the like, but not limited thereto.

The conductive material is used for imparting conductivity to the electrode. Any conductive material can be used without causing any chemical change in the battery. Examples of the conductive material include natural graphite, artificial graphite, carbon black, acetylene black, Metal powders such as black, carbon fiber, copper, nickel, aluminum, and silver, metal fibers, and the like, and conductive materials such as polyphenylene derivatives may be used alone or in combination.

The negative electrode and the positive electrode may be prepared by preparing an active material composition by mixing an active material, a binder and, optionally, a conductive material in a solvent, and applying the active material composition to each current collector. As the solvent, N-methylpyrrolidone or the like can be used, but it is not limited thereto. The method of manufacturing the electrode is well known in the art, and therefore, a detailed description thereof will be omitted herein.

The separator 113 separates the cathode 112 and the anode 114 and provides a passage for lithium ions. Any separator 113 may be used as long as it is commonly used in a lithium battery. That is, it is possible to use an electrolyte having a low resistance to ion movement and an excellent ability to impregnate an electrolyte. For example, selected from glass fiber, polyester, Teflon, polyethylene, polypropylene, polytetrafluoroethylene (PTFE), or a combination thereof, and may be nonwoven fabric or woven fabric. For example, a polyolefin-based polymer separator such as polyethylene, polypropylene and the like is mainly used for a lithium ion battery, and a coated separator containing a ceramic component or a polymer substance may be used for heat resistance or mechanical strength, Structure.

The lithium secondary battery can be classified into a lithium ion battery, a lithium ion polymer battery, and a lithium polymer battery according to the type of the separator and electrolyte used. The lithium secondary battery can be classified into a cylindrical shape, a square shape, a coin shape, Depending on the size, it can be divided into bulk type and thin type. The structure and the manufacturing method of these cells are well known in the art, and detailed description thereof will be omitted.

The electrolytic solution is as described above.

Hereinafter, the aspects of the present invention described above will be described in more detail through examples. However, the following examples are for illustrative purposes only and do not limit the scope of the invention.

Preparation of electrolytic solution

Manufacturing example  One

LiPF ₆ lithium salt was added to a mixed solvent of ethylene carbonate (EC), ethyl methyl carbonate (EMC) and dimethyl carbonate (DMC) in a volume ratio of 3/4/3 (v / v / v) 3-Methoxythiophene (MOT) was added in an amount of 0.2 wt% based on 100 wt% of the solution to prepare an electrolytic solution.

Manufacturing example  2

LiPF ₆ lithium salt was added to a mixed solvent of ethylene carbonate (EC), ethyl methyl carbonate (EMC) and dimethyl carbonate (DMC) in a volume ratio of 3/4/3 (v / v / v) 3-Methoxythiophene (MOT) was added in an amount of 0.008 wt% based on 100 wt% of the solution to prepare an electrolytic solution.

Manufacturing example  3

LiPF ₆ lithium salt was added to a mixed solvent of ethylene carbonate (EC), ethyl methyl carbonate (EMC) and dimethyl carbonate (DMC) in a volume ratio of 3/4/3 (v / v / v) Ethyl thiophene-3-acetate (ETA) was added in an amount of 0.14% by weight based on 100% by weight of the solution to prepare an electrolytic solution.

Manufacturing example  4

LiPF ₆ lithium salt was added to a mixed solvent of ethylene carbonate (EC), ethyl methyl carbonate (EMC) and dimethyl carbonate (DMC) in a volume ratio of 3/4/3 (v / v / v) Ethyl thiophene-3-acetate (ETA) was added in an amount of 0.008 wt% based on 100 wt% of the solution to prepare an electrolytic solution.

Manufacturing example  5

LiPF ₆ lithium salt was added to a mixed solvent of ethylene carbonate (EC), ethyl methyl carbonate (EMC) and dimethyl carbonate (DMC) in a volume ratio of 3/4/3 (v / v / v) Ethyl thiophene-3-acetate (ETA) was added in an amount of 0.01 wt% based on 100 wt% of the solution to prepare an electrolytic solution.

Comparative Manufacturing Example  One

LiPF ₆ lithium salt was added to a mixed solvent of ethylene carbonate (EC), ethyl methyl carbonate (EMC) and dimethyl carbonate (DMC) in a volume ratio of 3/4/3 (v / v / v) 3-Methylthiophene (MT) was added in an amount of 0.008% by weight based on 100% by weight of the solution to prepare an electrolytic solution.

Comparative Manufacturing Example  2

An electrolytic solution was prepared in the same manner as in Preparation Example 1, except that 3-methoxythiophene (MOT) was not included.

Preparation of lithium secondary battery 1

Example  One

LiNi _{0 .6} Co _{0 .2} using the positive electrode containing Mn _{0 .2} O ₂ and a lithium metal as the counter electrode using an electrolyte solution according to Preparation Example 1 was prepared (half cell) half cell.

Example  2

A half cell was prepared in the same manner as in Example 1, except that the electrolytic solution according to Production Example 2 was used in place of the electrolytic solution according to Preparation Example 1 above.

Example  3

A half cell was prepared in the same manner as in Example 1, except that the electrolytic solution according to Production Example 3 was used in place of the electrolytic solution according to Preparation Example 1 above.

Example  4

A half cell was prepared in the same manner as in Example 1, except that the electrolytic solution according to Preparation Example 4 was used in place of the electrolytic solution according to Preparation Example 1 above.

Example  5

A half cell was prepared in the same manner as in Example 1, except that the electrolytic solution according to Preparation Example 5 was used in place of the electrolytic solution according to Preparation Example 1 above.

Comparative Example  One

A half cell was produced in the same manner as in Example 1, except that the electrolytic solution according to Comparative Production Example 1 was used.

Comparative Example  2

A half cell was produced in the same manner as in Example 1, except that the electrolytic solution according to Comparative Production Example 2 was used.

Rating 1: passivation  Evaluation of film formation

After the half-cells according to Examples 3 and 4 and Comparative Examples 1 and 2 were charged and discharged once at 0.2 C, the formation of the passivation film was evaluated on the surface of the positive electrode.

The result will be described with reference to FIG.

FIG. 2 is a graph showing decomposition potentials of an electrolytic solution in a half-cell according to Examples 3 and 4 and Comparative Examples 1 and 2. FIG.

Referring to FIG. 2, the half-cell according to Examples 3 and 4 has decomposition potentials started at a lower voltage as compared with the half-cells according to Comparative Examples 1 and 2, and the passivation film can be easily formed on the surface of the anode .

Preparation of lithium secondary battery 2

Example  6

The anode is _{LiNi 0 .6 Co 0 .2 Mn 0} .2 O 2 , A negative electrode containing an alumina-coated graphite negative active material was used as a negative electrode, and a positive electrode active material prepared in Preparation Example 1 was used as a negative electrode. The coin cell (CR2016) was fabricated using the electrolyte solution.

Example  7

A coin cell (CR2016) was prepared in the same manner as in Example 6, except that the electrolytic solution according to Preparation Example 2 was used in place of the electrolytic solution according to Preparation Example 1 above.

Example  8

A coin cell (CR2016) was prepared in the same manner as in Example 6 except that the electrolytic solution according to Preparation Example 3 was used in place of the electrolytic solution according to Preparation Example 1. [

Example  9

A coin cell (CR2016) was prepared in the same manner as in Example 6, except that the electrolytic solution according to Production Example 4 was used in place of the electrolytic solution according to Production Example 1 above.

Comparative Example  3

A coin cell (CR2016) was prepared in the same manner as in Example 6, except that the electrolytic solution according to Comparative Preparation Example 1 was used.

Comparative Example  4

A coin cell (CR2016) was prepared in the same manner as in Example 6 except that the electrolytic solution according to Comparative Preparation Example 2 was used.

Evaluation 2: Life characteristics

Life characteristics of coin cells according to Examples 6 to 9 and Comparative Examples 3 and 4 were evaluated.

The coin cells according to Examples 6 to 9 and Comparative Examples 3 and 4 were subjected to charging and discharging at 200C or 80 times at 25 DEG C at 1 DEG C, and the discharge capacity according to each cycle was measured.

The results are shown in Figs. 3 to 5.

FIG. 3 is a graph showing capacity retention ratios according to cycles of a coin cell according to Example 6 and Comparative Example 4, FIG. 4 is a graph showing capacity retention ratios according to cycles of a coin cell according to Example 8 and Comparative Example 4, 5 is a graph showing the capacity retention rate according to cycles of coin cells according to Examples 7 and 9 and Comparative Examples 3 and 4;

3 to 5, it can be seen that the coin cells according to Examples 6 to 9 have higher capacity retention ratios according to cycles than the coin cells according to Comparative Examples 3 and 4, respectively.

Manufacture of lithium secondary battery 3

Example  10

The anode is _{.15 LiNi 0 .65 Co 0 Mn 0} .2 O 2 94wt%, Denka black (Denka black) and 3wt% of polyvinylidene fluoride (PVdF, Solef6020) was used to 3wt%, the platinum metal as the counter electrode And a half cell was produced using the electrolytic solution according to Production Example 5. [

Comparative Example  5

A half cell was prepared in the same manner as in Example 10, except that the electrolytic solution according to Comparative Preparation Example 1 was used.

Evaluation 3: Evaluation of electrochemical stability

The electrochemical stability characteristics of the coin cell according to Example 10 and Comparative Example 5 were evaluated.

The result is shown in Fig.

FIG. 6 shows the results of current changes according to the applied voltage of Example 10 and Comparative Example 5, and in Example 10, a sudden current change occurs in the region of 4.4 V or more. As a result, Quot ;. &lt; / RTI &gt; On the contrary, in Comparative Example 5, a sudden current change occurs in the region of 4.2 V, and the electrochemical stability is deteriorated in the region of 4.2 V or more.

While the present invention has been particularly shown and described with reference to exemplary embodiments thereof, it is to be understood that the invention is not limited to the disclosed exemplary embodiments, And falls within the scope of the invention.

100: Lithium secondary battery
112: cathode
113: Separator
114: anode
120: Battery container
140: sealing member

Claims (12)

delete delete delete delete Lithium salts;
Non-aqueous organic solvent; And
1. An electrolyte solution for a lithium secondary battery comprising an electrolyte additive represented by the following formula (2)
Wherein the electrolyte additive represented by the following Formula 2 is contained in an amount of 0.008 wt% to 0.2 wt% based on the total amount of the electrolyte for the lithium secondary battery:
(2)

In Formula 2,
R 'is a C1 to C12 alkyl group.
delete delete 6. The method of claim 5,
(2) is an electrolyte for a lithium secondary battery represented by the following formula (4): &lt; EMI ID =
[Chemical Formula 4]

.
delete delete A cathode comprising a cathode active material;
A negative electrode comprising a negative electrode active material; And
The electrolytic solution according to any one of claims 5 to 8,
&Lt; / RTI &gt;
12. The method of claim 11,
And a passivation film located on the surface of the anode.

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